JP7306961B2 - Adsorbent for basic amino acids - Google Patents

Adsorbent for basic amino acids Download PDF

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JP7306961B2
JP7306961B2 JP2019197815A JP2019197815A JP7306961B2 JP 7306961 B2 JP7306961 B2 JP 7306961B2 JP 2019197815 A JP2019197815 A JP 2019197815A JP 2019197815 A JP2019197815 A JP 2019197815A JP 7306961 B2 JP7306961 B2 JP 7306961B2
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basic amino
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大補 塚原
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Mizusawa Industrial Chemicals Ltd
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本発明は、新規な塩基性アミノ酸用吸着剤に関する。 TECHNICAL FIELD The present invention relates to a novel adsorbent for basic amino acids.

アルギニン、ヒスチジン及びリジンは、いずれも側鎖にアミノ基を有するアミノ酸であり、これらは塩基性アミノ酸と呼ばれている。 Arginine, histidine and lysine are all amino acids having amino groups in their side chains and are called basic amino acids.

塩基性アミノ酸は、苦みを呈する成分として知られており、調味料や飲料などの風味改善のためには、塩基性アミノ酸を選択的に分離・除去することが望まれる。 Basic amino acids are known to be bitter-tasting components, and it is desired to selectively separate and remove basic amino acids in order to improve the flavor of seasonings and beverages.

しかし、粘土鉱物によりアミノ酸溶液から不純物を除去する技術(特許文献1参照)や、アミノ酸を粘土鉱物に担持する技術(特許文献2参照)は検討されているものの(特許文献1参照)、複数種類のアミノ酸を含有する溶液から特定のアミノ酸を選択的に吸着する技術についてはほとんど検討されていないのが実情である。 However, although a technique for removing impurities from an amino acid solution using clay minerals (see Patent Document 1) and a technique for supporting amino acids on clay minerals (see Patent Document 2) have been investigated (see Patent Document 1), there are several types of In fact, almost no studies have been made on techniques for selectively adsorbing a specific amino acid from a solution containing such amino acids.

特開2005-104959号Japanese Patent Application Laid-Open No. 2005-104959 特開昭62-270536号JP-A-62-270536

本発明の目的は、塩基性アミノ酸を含有する溶液から塩基性アミノ酸を選択的に吸着し得る吸着剤を提供することにある。 An object of the present invention is to provide an adsorbent capable of selectively adsorbing a basic amino acid from a solution containing the basic amino acid.

本発明によれば、ジオクタヘドラル型スメクタイト系粘土からなる塩基性アミノ酸用吸着剤であって、前記ジオクタヘドラル型スメクタイト系粘土のSiO/Al比が10以下であることを特徴とする塩基性アミノ酸用吸着剤が提供される。 According to the present invention, there is provided an adsorbent for basic amino acids comprising a dioctahedral smectite clay, wherein the dioctahedral smectite clay has a SiO 2 /Al 2 O 3 ratio of 10 or less. A sorbent for amino acids is provided.

本発明の塩基性アミノ酸用吸着剤においては、
(1)前記ジオクタヘドラル型スメクタイト系粘土のHo≦-3.0の固体酸量が0.10mmol/g-dry clay以上であること、
(2)前記ジオクタヘドラル型スメクタイト系粘土のカチオン交換容量が20mmol/100g以上であること、
(3)前記ジオクタヘドラル型スメクタイト系粘土が酸処理物であること、
(4)前記ジオクタヘドラル型スメクタイト系粘土のSiO/Al比が7.5以下であること、
(5)前記塩基性アミノ酸がアルギニン又はヒスチジンであること、
が好適である。
In the adsorbent for basic amino acids of the present invention,
(1) The dioctahedral smectite clay has a solid acid amount of Ho≦−3.0 of 0.10 mmol/g-dry clay or more;
(2) the dioctahedral smectite clay has a cation exchange capacity of 20 mmol/100 g or more;
(3) the dioctahedral smectite clay is acid-treated;
(4) the dioctahedral smectite clay has a SiO 2 /Al 2 O 3 ratio of 7.5 or less;
(5) the basic amino acid is arginine or histidine;
is preferred.

本発明において塩基性アミノ酸吸着剤として用いられるジオクタヘドラル型スメクタイト系粘土は、SiO/Al比(質量比)が調整されている結果、塩基性アミノ酸を選択的に吸着することができる。 The dioctahedral smectite clay used as a basic amino acid adsorbent in the present invention can selectively adsorb basic amino acids as a result of its adjusted SiO 2 /Al 2 O 3 ratio (mass ratio).

本発明の塩基性アミノ酸用吸着剤は、SiO/Al比(質量比)が10以下、好ましくは7.5以下のジオクタヘドラル型スメクタイト系粘土から成ることを特徴とするが、SiO/Al比が当該範囲にあることに由来して、比較的強い固体酸性を示す。 The adsorbent for basic amino acids of the present invention is characterized by comprising a dioctahedral smectite clay having a SiO 2 /Al 2 O 3 ratio (mass ratio) of 10 or less , preferably 7.5 or less. Since the /Al 2 O 3 ratio is within the range, it exhibits relatively strong solid acidity.

例えば、前記ジオクタヘドラル型スメクタイト系粘土のHo≦-3.0の固体酸量は、0.10mmol/g-dry clay以上が好適であり、0.20mmol/g-dry clay以上がより好適であり、0.70mmol/g-dry clay以上が最も好適である。 For example, the dioctahedral smectite clay has a solid acid amount of Ho ≤ -3.0 that is preferably 0.10 mmol/g-dry clay or more, more preferably 0.20 mmol/g-dry clay or more, 0.70 mmol/g-dry clay or more is most preferred.

このように前記ジオクタヘドラル型スメクタイト系粘土は比較的強い固体酸性を示すが、このことが、塩基性アミノ酸に対する優れた吸着性能を発揮する一因であるものと推察される。
即ち、塩基性アミノ酸は2つのアミノ基と1つのカルボン酸基を有するため、水溶液中では、陽イオン(2価)、陽イオン(1価)、双生イオン及び陰イオン(1価)が平衡状態にあり、水溶液中のpH変化にしたがって平衡が移動する。
例えば、高pH(塩基性)条件下ではカルボン酸が陰イオンとなるため、平衡は陰イオン側に傾いている。ここに、比較的強い固体酸を含んでいる本発明の吸着剤を水溶液中に添加していくと、pHが下がり、アミノ基が陽イオンとなり、塩基性アミノ酸の平衡は陽イオン側に移動する。従って、この塩基性アミノ酸の陽イオンが前記ジオクタヘドラル型スメクタイト系粘土の層間に有する負電荷により捕捉され、この結果、塩基性アミノ酸の吸着性が発現することとなる。
As described above, the dioctahedral-type smectite clay exhibits relatively strong solid acidity, which is presumed to be one of the reasons for its excellent adsorption performance for basic amino acids.
That is, since a basic amino acid has two amino groups and one carboxylic acid group, cations (divalent), cations (monovalent), zwitterions and anions (monovalent) are in equilibrium in an aqueous solution. , and the equilibrium shifts as the pH of the aqueous solution changes.
For example, under high pH (basic) conditions, the carboxylic acid becomes an anion, so the equilibrium is tilted towards the anion side. Here, when the adsorbent of the present invention containing a relatively strong solid acid is added to the aqueous solution, the pH decreases, the amino groups become cations, and the equilibrium of basic amino acids shifts to the cation side. . Therefore, the cation of this basic amino acid is captured by the negative charge between the layers of the dioctahedral smectite clay, and as a result, the adsorption of the basic amino acid is exhibited.

前記ジオクタヘドラル型スメクタイト系粘土のAl比率は、9質量%以上が好適であり、14質量%以上がより好適である。 The Al 2 O 3 ratio of the dioctahedral smectite clay is preferably 9% by mass or more, more preferably 14% by mass or more.

前記ジオクタヘドラル型スメクタイト系粘土のカチオン交換容量(CEC)は、20mmol/100g以上が好適であり、40mmol/100g以上がより好適であり、50mmol/100g以上が最も好適である。 The cation exchange capacity (CEC) of the dioctahedral smectite clay is preferably 20 mmol/100 g or more, more preferably 40 mmol/100 g or more, and most preferably 50 mmol/100 g or more.

ここで、ジオクタヘドラル型スメクタイト系粘土について説明する。
ジオクタヘドラル型スメクタイト系粘土は、SiO四面体層-AlO八面体層-SiO四面体層からなり、且つこれらの四面体層と八面体層が部分的に異種金属で同形置換された三層構造を基本構造(単位層)としており、このような三層構造の積層層間には、Ca、K、Na等の金属陽イオンや水素イオンとそれに配位している水分子が存在している。また、基本三層構造の八面体層中のAlの一部にMgやFe(II)が置換し、四面体層中のSiの一部にAlが置換しているため、結晶格子はマイナスの電荷を有しており、このマイナスの電荷が基本層間に存在する金属陽イオンや水素イオンにより中和されている。
The dioctahedral smectite clay will now be described.
Dioctahedral-type smectite clay consists of SiO 4 tetrahedral layer-AlO 6 octahedral layer-SiO 4 tetrahedral layer, and these tetrahedral layers and octahedral layers are partially isomorphically substituted with dissimilar metals. The structure is a basic structure (unit layer), and metal cations such as Ca, K, Na, etc. and hydrogen ions and water molecules coordinated with them are present between the laminated layers of such a three-layer structure. . In addition, Mg and Fe (II) are substituted for part of Al in the octahedral layer of the basic three-layer structure, and Al is substituted for part of Si in the tetrahedral layer, so the crystal lattice is negative. It has an electric charge, and this negative electric charge is neutralized by metal cations and hydrogen ions existing between the basic layers.

このようなジオクタヘドラル型スメクタイト系粘土には、酸性白土、ベントナイト、フラーズアース等があり、基本層間に存在する金属陽イオンの種類や量、及び水素イオン量等によってそれぞれ異なる特性を示す。例えば、ベントナイトでは、基本層間に存在するNaイオン量が多く、このため、水に懸濁分散させた分散液のpHが高くなる。一方、酸性白土では、基本層間に存在する水素イオン量が多く、このため、水に懸濁分散させた分散液のpHが低くなる。 Such dioctahedral smectite clays include acid clay, bentonite, Fraser's earth, etc., and exhibit different characteristics depending on the type and amount of metal cations present between the basic layers, the amount of hydrogen ions, and the like. For example, in bentonite, a large amount of Na ions exist between the basic layers, so that the pH of the dispersion liquid suspended and dispersed in water becomes high. On the other hand, in acid clay, the amount of hydrogen ions present between the basic layers is large, so that the pH of the dispersion liquid suspended and dispersed in water is low.

また、かかるジオクタヘドラル型スメクタイト系粘土は、粘土の成因、産地及び同じ産地でも埋蔵場所(切羽)等によっても相違するが、一般的には、酸化物換算で以下のような組成を有している。
SiO;50~75質量%
Al;11~25質量%
Fe;2~20質量%
MgO;2~7質量%
CaO;0.1~3質量%
NaO;0.1~3質量%
O;0.1~3質量%
その他の酸化物(TiO等);2質量%以下
Ig-loss(1050℃);5~11質量%
In addition, such dioctahedral smectite clay varies depending on the origin of the clay, the place of production, and even in the same place of production, the burial place (face), etc., but in general, it has the following composition in terms of oxide. .
SiO 2 ; 50 to 75% by mass
Al 2 O 3 ; 11 to 25% by mass
Fe 2 O 3 ; 2 to 20% by mass
MgO; 2 to 7% by mass
CaO; 0.1 to 3% by mass
Na 2 O; 0.1 to 3% by mass
K 2 O; 0.1 to 3% by mass
Other oxides (TiO 2, etc.); 2% by mass or less Ig-loss (1050°C); 5 to 11% by mass

前記ジオクタヘドラル型スメクタイト系粘土は、産地等によっては、石英等の不純物を多く含んでいることもある。従って、必要により石砂分離、浮力選鉱、磁力選鉱、水簸、風簸等の精製操作に賦して不純物をできるだけ除去した後に用いるのがよい。 The dioctahedral smectite clay may contain a large amount of impurities such as quartz depending on the place of production. Therefore, it is preferable to remove impurities as much as possible by performing refining operations such as sand separation, flotation beneficiation, magnetic beneficiation, elutriation, and air elutriation, if necessary, before use.

本発明で塩基性アミノ酸吸着剤として使用するジオクタヘドラル型スメクタイト系粘土は、特に限定されるものではないが、酸性白土を使用することが好適である。 The dioctahedral smectite clay used as the basic amino acid adsorbent in the present invention is not particularly limited, but acid clay is preferably used.

また、本発明の塩基性アミノ酸吸着剤としてとしては、酸性白土を酸処理したものを使用することがより好適である。この酸処理物は、活性白土と称されるものであり、ジオクタヘドラル型スメクタイト系粘土の基本層構造を破壊しない程度に酸処理したものである。酸処理により多孔度が上がるため、種々の物質の吸着に有利となる。 Moreover, as the basic amino acid adsorbent of the present invention, it is more preferable to use an acid-treated acid clay. This acid-treated product is called activated clay, and is acid-treated to such an extent that the basic layer structure of the dioctahedral smectite clay is not destroyed. Acid treatment increases porosity, which is advantageous for adsorption of various substances.

上記のような特性を有する活性白土は、夾雑物が取り除かれた酸性白土を所定の条件で酸処理することで製造される。
酸処理条件は、目的とする活性白土の物性(固体酸量など)に応じて適宜設定すればよく、例えば硫酸水溶液を使用する場合には、原料粘土中に含まれる水分も硫酸水溶液を構成するものとして算出した硫酸水溶液量が、通常、原料粘土100質量部(110℃乾燥物として)当り250~800質量部、その時の硫酸水溶液の濃度が15~45質量%になるような条件で行えばよい。
The activated clay having the properties as described above is produced by acid-treating the acid clay from which contaminants have been removed under predetermined conditions.
The acid treatment conditions may be appropriately set according to the physical properties (solid acid content, etc.) of the desired activated clay. For example, when using an aqueous sulfuric acid solution, the water contained in the starting clay also constitutes the aqueous sulfuric acid solution. The amount of sulfuric acid aqueous solution calculated as a substance is usually 250 to 800 parts by mass per 100 parts by mass of raw clay (110 ° C dry matter), and the concentration of the sulfuric acid aqueous solution at that time is 15 to 45% by mass. good.

さらに、本発明の塩基性アミノ酸吸着剤としてとしては、酸性白土を弱酸処理したものを使用することが特に好適である。以下、このような酸処理物を弱酸処理白土と呼ぶ。
かかる弱酸処理白土は、活性白土に比して弱い酸処理で得られるため、固体酸点として働くAlやMgの溶出が抑えられている。その一方で、固体酸点として働くAlやMgを覆っているNa分やCa分は除去されている。ゆえに、活性白土あるいは酸性白土に比して同等以上の固体酸量を示す。
Furthermore, as the basic amino acid adsorbent of the present invention, it is particularly preferable to use acid clay treated with a weak acid. Such an acid-treated product is hereinafter referred to as weak acid-treated clay.
Such weak acid-treated clay is obtained by a weaker acid treatment than activated clay, so the elution of Al and Mg, which act as solid acid sites, is suppressed. On the other hand, Na and Ca covering Al and Mg acting as solid acid sites are removed. Therefore, it exhibits a solid acid content equal to or greater than that of activated clay or acid clay.

このような弱酸処理白土のSiO/Al比(質量比)は、7.5以下が好適である。 The SiO 2 /Al 2 O 3 ratio (mass ratio) of such weak acid-treated clay is preferably 7.5 or less.

このような弱酸処理白土のHo≦-3.0の固体酸量は、0.70mmol/g-dry clay以上が好適である。 The solid acid content of such weakly acid-treated clay with Ho≦−3.0 is preferably 0.70 mmol/g-dry clay or more.

このような弱酸処理白土のAl比率は、14質量%以上が好適である。 The Al 2 O 3 ratio of such weak acid-treated clay is preferably 14% by mass or more.

上記のような特性を有する弱酸処理白土は、夾雑物が取り除かれた酸性白土を所定の条件で弱酸処理することにより製造される。
かかる弱酸処理は、従来公知の活性白土や半活性白土を製造する際の酸処理に比してマイルドな条件下で行われる。例えば硫酸水溶液を使用する場合には、原料粘土中に含まれる水分も硫酸水溶液を構成するものとして算出した硫酸水溶液量が、原料粘土100質量部(110℃乾燥物として)当り250~800質量部、その時の硫酸水溶液の濃度が1~15質量%程度になるような条件で酸処理を行えばよい。酸処理にあたっては、必要により25~95℃程度に加熱することもできる。このようにして、原料の組成、用いる酸水溶液の酸濃度、処理温度等によって、SiO/Al比が所定の範囲となる程度の時間(0.5~12時間程度、好ましくは0.5~8時間程度、特に好ましくは0.5~4時間程度)、酸処理を行えばよい。
The weak acid-treated clay having the properties as described above is produced by subjecting acid clay from which contaminants have been removed to weak acid treatment under predetermined conditions.
Such a weak acid treatment is carried out under milder conditions than the acid treatment for producing conventionally known activated clay or semi-activated clay. For example, when an aqueous sulfuric acid solution is used, the amount of the aqueous sulfuric acid solution, calculated assuming that the water contained in the raw material clay also constitutes the aqueous sulfuric acid solution, is 250 to 800 parts by mass per 100 parts by mass of the raw clay (110° C. dry matter). , the acid treatment may be performed under such conditions that the concentration of the sulfuric acid aqueous solution at that time is about 1 to 15% by mass. In the acid treatment, heating to about 25 to 95° C. can be carried out if necessary. In this way, depending on the composition of the raw material, the acid concentration of the acid aqueous solution used, the treatment temperature, etc., the time required for the SiO 2 /Al 2 O 3 ratio to be within a predetermined range (about 0.5 to 12 hours, preferably 0 0.5 to 8 hours, particularly preferably 0.5 to 4 hours).

本発明の吸着剤は、塩基性アミノ酸を含有する溶液から塩基性アミノ酸を選択的に吸着することができる。 The adsorbent of the present invention can selectively adsorb basic amino acids from solutions containing basic amino acids.

本発明の吸着剤は、塩基性アミノ酸の中でも、アルギニン又はヒスチジンを好適に吸着することができる。 The adsorbent of the present invention can preferably adsorb arginine or histidine among basic amino acids.

本発明の吸着剤により調味料や飲料から塩基性アミノ酸を選択的に除去することで、塩基性アミノ酸由来の苦みを低減させることができる。例えば、醤油、味噌、魚介エキス、肉エキス又は酵母エキスなどの調味料や、アミノ酸含有の機能性飲料などの苦み低減に利用することができる。 By selectively removing basic amino acids from seasonings and beverages with the adsorbent of the present invention, bitterness derived from basic amino acids can be reduced. For example, it can be used to reduce the bitterness of seasonings such as soy sauce, miso, seafood extract, meat extract or yeast extract, and amino acid-containing functional beverages.

また、本発明の吸着剤は、吸着した塩基性アミノ酸を適宜溶媒で抽出・精製し利用することもできる。 The adsorbent of the present invention can also be used by extracting and purifying the adsorbed basic amino acid with an appropriate solvent.

本発明の吸着剤は、溶液に含有される塩基性アミノ酸1質量部あたり0.1~100質量部以上、好ましくは1~10質量部の量で使用される。この投入量が少ないと、当然のことながら、塩基性アミノ酸の吸着量が不十分となってしまう。また、投入量が必要以上に多い場合には、コストの点で不利となってしまう。 The adsorbent of the present invention is used in an amount of 0.1 to 100 parts by weight or more, preferably 1 to 10 parts by weight, per 1 part by weight of the basic amino acid contained in the solution. If the input amount is small, the amount of adsorption of the basic amino acid will naturally be insufficient. In addition, if the amount to be charged is larger than necessary, it is disadvantageous in terms of cost.

塩基性アミノ酸を吸着した本発明の吸着剤は、遠心分離や濾過等公知の方法により分離され、取り出される。分離の方法としては、有効成分のロスが少ないという観点から、濾過が好ましい。 The adsorbent of the present invention that has adsorbed basic amino acids is separated and taken out by a known method such as centrifugation or filtration. Filtration is preferable as the separation method from the viewpoint of less loss of the active ingredient.

本発明の優れた効果を、次の実施例により説明する。 The excellent effects of the present invention are illustrated by the following examples.

(実施例1)
新潟県胎内市産のジオクタヘドラル型スメクタイト系粘土ペレット700gを90℃に加熱した5質量%硫酸水溶液1000mlに投入した。液温90℃に維持した状態で撹拌し、30分間酸処理を行った。酸処理終了後、水で洗浄したペレットを110℃にて乾燥し、粉砕、分級して弱酸処理白土粉末を得た。
(Example 1)
700 g of dioctahedral smectite clay pellets from Tainai City, Niigata Prefecture were put into 1000 ml of a 5% by mass sulfuric acid aqueous solution heated to 90°C. The mixture was stirred while maintaining the liquid temperature at 90° C., and acid treatment was performed for 30 minutes. After acid treatment, the pellets washed with water were dried at 110° C., pulverized and classified to obtain weakly acid-treated clay powder.

(実施例2)
水澤化学工業(株)製活性白土(A)
(Example 2)
Activated clay (A) manufactured by Mizusawa Chemical Industry Co., Ltd.

(実施例3)
水澤化学工業(株)製酸性白土
(Example 3)
Acid clay manufactured by Mizusawa Chemical Industry Co., Ltd.

(比較例1)
水澤化学工業(株)製活性白土(B)
(Comparative example 1)
Activated clay (B) manufactured by Mizusawa Chemical Industry Co., Ltd.

(1)元素分析
元素分析については、(株)リガク社製Rigaku ZSX primus IIを用い、定量ソフトEzスキャンにより各元素の酸化物量(質量%)の測定を行った。
(1) Elemental Analysis For elemental analysis, Rigaku ZSX primus II manufactured by Rigaku Co., Ltd. was used to measure the oxide amount (% by mass) of each element by quantitative software Ez scan.

(2)カチオン交換容量
ショーレンベルガー法に準拠し試料100g当たりのカチオン交換容量を測定した(参考文献「日本ベントナイト工業会標準試験方法」)。結果を表1に示す。
(2) Cation Exchange Capacity The cation exchange capacity per 100 g of sample was measured according to the Schöllenberger method (reference document "Japan Bentonite Industry Association Standard Test Method"). Table 1 shows the results.

(3)固体酸量
n-ブチルアミン滴定法にてHo≦-3.0の固体酸量を測定した。尚、試料はあらかじめ150℃で3時間乾燥したものを用いた{参考文献:「触媒」Vol.11,No6,P210-216(1969)}。結果を表1に示す。
(3) Solid acid content A solid acid content of Ho≤-3.0 was measured by n-butylamine titration method. The sample used was previously dried at 150° C. for 3 hours {Reference: “Catalyst” Vol. 11, No. 6, P210-216 (1969)}. Table 1 shows the results.

(4)pH
イオン交換水に試料濃度が5質量%になるように吸着剤粉末を添加し、30分間撹拌した後、東亜ディーケーケー製pHメーターHM-30Rにて測定を行った。結果を表1に示す。
(4) pH
Adsorbent powder was added to ion-exchanged water so that the sample concentration was 5% by mass, and after stirring for 30 minutes, the pH was measured with a pH meter HM-30R manufactured by DKK Toa. Table 1 shows the results.

(5)吸着試験
富士フイルム和光純薬(株)製アミノ酸混合標準液(H型)5mlに対して試料0.05gを投入し振盪した後、冷蔵庫内に静置した。10分おきに冷蔵庫から取り出して振盪し、合計30分間静置したところで、上澄みをメンブランフィルター(アドバンテック製、フィルター孔径0.45μm)で濾過し、試料液を得た。得られた試料液についてアミノ酸自動分析計により、試料液100gあたりの各アミノ酸の含有量(mg)を測定した。結果を表2に示す。尚、カッコ内は未処理標準液とのアミノ酸含有量(mg)の差である。
(5) Adsorption Test 0.05 g of a sample was added to 5 ml of an amino acid mixed standard solution (H-type) manufactured by Fuji Film Wako Pure Chemical Industries, Ltd., shaken, and then allowed to stand in a refrigerator. It was taken out from the refrigerator every 10 minutes, shaken, and allowed to stand for a total of 30 minutes, and then the supernatant was filtered through a membrane filter (manufactured by Advantech, filter pore size 0.45 μm) to obtain a sample solution. The content (mg) of each amino acid per 100 g of the sample solution was measured with an amino acid automatic analyzer for the obtained sample solution. Table 2 shows the results. The value in parentheses is the difference in amino acid content (mg) from the untreated standard solution.

Figure 0007306961000001
Figure 0007306961000001

Figure 0007306961000002
Figure 0007306961000002

Claims (6)

ジオクタヘドラル型スメクタイト系粘土からなる塩基性アミノ酸用吸着剤であって、
前記ジオクタヘドラル型スメクタイト系粘土のSiO/Al比が10以下であることを特徴とする塩基性アミノ酸用吸着剤。
An adsorbent for basic amino acids made of dioctahedral smectite clay,
An adsorbent for basic amino acids, wherein the dioctahedral smectite clay has a SiO 2 /Al 2 O 3 ratio of 10 or less.
前記ジオクタヘドラル型スメクタイト系粘土のHo≦-3.0の固体酸量が0.10mmol/g-dry clay以上である請求項1に記載の塩基性アミノ酸用吸着剤。 2. The adsorbent for basic amino acids according to claim 1, wherein the dioctahedral smectite clay has a solid acid content of Ho≤-3.0 of 0.10 mmol/g-dry clay or more. 前記ジオクタヘドラル型スメクタイト系粘土のカチオン交換容量が20mmol/100g以上である請求項1又は2に記載の塩基性アミノ酸用吸着剤。 3. The adsorbent for basic amino acids according to claim 1, wherein the dioctahedral smectite clay has a cation exchange capacity of 20 mmol/100 g or more. 前記ジオクタヘドラル型スメクタイト系粘土が酸処理物である請求項1~3の何れかに記載の塩基性アミノ酸用吸着剤。 The adsorbent for basic amino acids according to any one of claims 1 to 3, wherein the dioctahedral smectite clay is acid-treated. 前記ジオクタヘドラル型スメクタイト系粘土のSiO/Al比が7.5以下である請求項1~4の何れかに記載の塩基性アミノ酸用吸着剤。 The adsorbent for basic amino acids according to any one of claims 1 to 4, wherein the dioctahedral smectite clay has a SiO 2 /Al 2 O 3 ratio of 7.5 or less. 前記塩基性アミノ酸がアルギニン又はヒスチジンである請求項1~5の何れかに記載の塩基性アミノ酸用吸着剤。 The adsorbent for basic amino acids according to any one of claims 1 to 5, wherein said basic amino acid is arginine or histidine.
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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000344513A (en) 1999-06-01 2000-12-12 Mizusawa Ind Chem Ltd Activated clay shaped particle, its production and its utilization
JP2005104959A (en) 2003-01-23 2005-04-21 Nippon Soda Co Ltd Agricultural and horticultural water dispersible granule
US20060276333A1 (en) 2003-05-25 2006-12-07 Ulrich Sohling Agent for adsorbing protein from protein-containing liquids in the foood sector
JP2010011858A (en) 2009-09-03 2010-01-21 Kao Corp Tea extract
JP2017136584A (en) 2016-01-28 2017-08-10 水澤化学工業株式会社 Absorbent for purine body

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JPH10182142A (en) * 1996-10-23 1998-07-07 Osaki Kogyo Kk Metallic fine particle/solid carrier composition, its use and production

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000344513A (en) 1999-06-01 2000-12-12 Mizusawa Ind Chem Ltd Activated clay shaped particle, its production and its utilization
JP2005104959A (en) 2003-01-23 2005-04-21 Nippon Soda Co Ltd Agricultural and horticultural water dispersible granule
US20060276333A1 (en) 2003-05-25 2006-12-07 Ulrich Sohling Agent for adsorbing protein from protein-containing liquids in the foood sector
JP2010011858A (en) 2009-09-03 2010-01-21 Kao Corp Tea extract
JP2017136584A (en) 2016-01-28 2017-08-10 水澤化学工業株式会社 Absorbent for purine body

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